NDC 0004-6416 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0004-6416 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020067 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1994-10-14 |
Marketing End Date | 2018-07-31 |